WO2016121371A1 - Case hardened steel - Google Patents
Case hardened steel Download PDFInfo
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- WO2016121371A1 WO2016121371A1 PCT/JP2016/000359 JP2016000359W WO2016121371A1 WO 2016121371 A1 WO2016121371 A1 WO 2016121371A1 JP 2016000359 W JP2016000359 W JP 2016000359W WO 2016121371 A1 WO2016121371 A1 WO 2016121371A1
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- fatigue strength
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- 229910000760 Hardened steel Inorganic materials 0.000 title claims abstract description 11
- 229910000831 Steel Inorganic materials 0.000 claims description 46
- 239000010959 steel Substances 0.000 claims description 46
- 239000012535 impurity Substances 0.000 claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 9
- 239000000203 mixture Substances 0.000 abstract description 8
- 238000005452 bending Methods 0.000 description 31
- 230000000052 comparative effect Effects 0.000 description 20
- 239000010410 layer Substances 0.000 description 20
- 230000000694 effects Effects 0.000 description 18
- 230000002829 reductive effect Effects 0.000 description 18
- 238000005255 carburizing Methods 0.000 description 17
- 239000002344 surface layer Substances 0.000 description 13
- 230000003247 decreasing effect Effects 0.000 description 11
- 239000006104 solid solution Substances 0.000 description 11
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 10
- 229910052804 chromium Inorganic materials 0.000 description 10
- 230000007423 decrease Effects 0.000 description 9
- 229910052710 silicon Inorganic materials 0.000 description 9
- 230000002159 abnormal effect Effects 0.000 description 8
- 238000010791 quenching Methods 0.000 description 8
- 230000000171 quenching effect Effects 0.000 description 8
- 239000013078 crystal Substances 0.000 description 7
- 238000009661 fatigue test Methods 0.000 description 7
- 229910052748 manganese Inorganic materials 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 238000005496 tempering Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 229910001566 austenite Inorganic materials 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 230000000717 retained effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229910000712 Boron steel Inorganic materials 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000005242 forging Methods 0.000 description 3
- 238000005121 nitriding Methods 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000010502 deborylation reaction Methods 0.000 description 2
- 238000005261 decarburization Methods 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 238000010606 normalization Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
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- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910011214 Ti—Mo Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000005256 carbonitriding Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
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- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 238000005480 shot peening Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000010421 standard material Substances 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/32—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for gear wheels, worm wheels, or the like
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/06—Surface hardening
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/26—Methods of annealing
- C21D1/28—Normalising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/002—Heat treatment of ferrous alloys containing Cr
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/008—Heat treatment of ferrous alloys containing Si
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/32—Ferrous alloys, e.g. steel alloys containing chromium with boron
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/08—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
- C23C8/20—Carburising
- C23C8/22—Carburising of ferrous surfaces
Definitions
- the present invention relates to a case-hardened steel used by carburizing and quenching, and in particular, a boron-containing case-hardened steel excellent in fatigue resistance and impact resistance, which can be applied to drive transmission parts such as automobiles.
- surface hardening heat treatments such as carburizing, nitriding, and carbonitriding are performed on parts that require high fatigue strength and wear resistance in machine parts used as automobiles, construction machines, and other various industrial machines.
- case-hardened steel such as SCr, SCM, SNCM, etc. is usually used in JIS standards, and after forming into the desired part shape by machining such as forging or cutting, the above-mentioned surface hardening heat treatment is applied. Then, it is manufactured into parts through a finishing process such as polishing.
- Patent Document 1 discloses a case-hardened boron steel that can suppress the coarsening of crystal grains with TiN while adding Ti to fix N in the form of TiN and securing solid solution B. .
- Patent Document 2 proposes to improve toughness by adjusting the addition amount of Si, Mn and Cr in the Ti-added boron steel and reducing the carburizing abnormal layer depth.
- Patent Document 3 discloses a method for producing a case-hardened boron steel that suppresses the formation of BN by adding a large amount of Al and prevents abnormal grain growth of fine grains by fine carbonitride obtained by heat treatment before carburizing. It is disclosed.
- Patent Document 4 discloses a case hardening steel excellent in cold forgeability that suppresses the occurrence of an abnormal carburizing layer by addition of Sb and effectively suppresses coarsening of crystal grains by Ti-Mo carbide. Is disclosed. Further, Patent Document 5 discloses a steel for machine structural use that suppresses the thickness of the decarburized layer by adding Sb and has a cold workability equivalent to that of a steel material that has been subjected to conventional soft annealing, and a method for manufacturing the same. .
- JP-A-57-070261 JP 58-120719 A Japanese Patent Laid-Open No. 2003-342635 JP 2012-62536 A Japanese Patent Laid-Open No. 2004-250767
- each of the inventions described in Patent Documents 1 to 4 has the following problems.
- N is fixed in the form of TiN, and it is considered that B does not combine with N.
- TiN exists in steel as a relatively large square inclusion, this becomes a starting point of fatigue, and in gears, surface fatigue such as pitching and bending fatigue strength at the root are reduced.
- the square TiN reduces the impact resistance of the gear and may cause breakage of the gear when an impact load is applied to the gear.
- Patent Document 5 depending on the balance between Sb having a decarburization-inhibiting effect and Si that promotes decarburization, it is difficult to reliably avoid the reduction of carbon on the surface layer, and desired characteristics can be obtained. There is a problem that can not be.
- an object of the present invention is to solve the above-described problems and to provide a case-hardened steel having excellent fatigue characteristics at a relatively low production cost.
- the present invention is based on the above findings. That is, the gist configuration of the present invention is as follows. 1. % By mass C: 0.10 to 0.30%, Si: 0.10 to 1.20% Mn: 0.30-1.50% S: 0.010 to 0.030%, Cr: 0.10 to 1.00%, B: 0.0005-0.0050%, Sb: 0.005 to 0.020% and N: 0.0150% or less are included within a range satisfying the following formula, When B- (10.8 / 14) N ⁇ 0.0003%, 0.010% ⁇ Al ⁇ 0.120% and B- (10.8 / 14) N ⁇ 0.0003%, 27/14 [((N ⁇ (14 / 10.8 ) B + 0.030] ⁇ Al ⁇ 0.120%, the balance is iron and inevitable impurities, Ti in the inevitable impurities, Ti: Case-hardened steel characterized by being 0.005% or less. Sb ⁇ ⁇ Si / 2 + (Mn + Cr) / 5 ⁇ / 70
- C 0.10 to 0.30%
- C 0.10 to 0.30%
- the toughness of the core part decreases. Therefore, the C content is limited to the range of 0.10 to 0.30%. Preferably it is 0.15 to 0.25% of range.
- Si 0.10 to 1.20%
- Si is an element effective for increasing the softening resistance in a temperature range of 200 to 300 ° C., which is estimated to be reached during rolling of gears and the like. It also has an effect of suppressing the formation of coarse carbides during carburization, and at least 0.10% addition is essential.
- Si is a ferrite stabilizing element, and excessive addition raises the Ac 3 transformation point, and in the normal quenching temperature range, ferrite tends to appear in the core portion having a low carbon content, and at the tooth base. Since the bending fatigue strength decreases, the upper limit was made 1.20%. Preferably it is 0.20 to 0.60% of range.
- Mn 0.30 to 1.50%
- Mn is an element effective for improving the hardenability and needs to be added at least 0.30%.
- Mn tends to form an abnormal carburization layer, and excessive addition causes an excessive amount of retained austenite and leads to a decrease in hardness, so the upper limit was made 1.50%.
- the upper limit was made 1.50%.
- it is 0.50 to 1.20% of range.
- S 0.010-0.030% S has a function of forming sulfides with Mn and improving machinability, so it is contained at least 0.010% or more. On the other hand, excessive addition reduces the fatigue strength and toughness of the parts, so the upper limit was made 0.030%.
- Cr 0.10 to 1.00% Cr is an element effective for improving not only hardenability but also temper softening resistance, and if the content is less than 0.10%, its addition effect is poor. On the other hand, when it exceeds 1.00%, it becomes easy to form a carburized abnormal layer. Further, the hardenability becomes too high, the toughness inside the gear is deteriorated, and the bending fatigue strength is lowered. Therefore, the Cr content is limited to the range of 0.10 to 1.00%. Preferably it is 0.10 to 0.60% of range.
- B 0.0005-0.0050%
- B is an element effective for ensuring hardenability by adding a small amount, and needs to be added at least 0.0005%.
- the amount of B is limited to the range of 0.0005 to 0.0050%. Preferably it is 0.0010 to 0.0040% of range.
- Sb 0.005-0.020% Since Sb has a strong tendency to segregate at grain boundaries, Sb is an important element for suppressing surface reaction such as deboronization and nitriding (BN formation) during carburizing treatment and ensuring hardenability. In order to obtain the effect, the addition of at least 0.005% is essential. However, excessive addition not only leads to an increase in cost but also reduces toughness, so the upper limit was made 0.020%. Preferably it is 0.005 to 0.015% of range.
- the hardness is lowered with a decrease in the hardenability in the peripheral portion, and fatigue failure starting from the hardness tends to occur.
- the lower limit of the amount of Sb having the effect of suppressing grain boundary oxidation as indicated by the right side of the above formula according to the content of Si, Mn, Cr, ensuring hardenability in the surface layer It is possible to suppress a decrease in fatigue strength.
- N 0.0150% or less N is an element that combines with Al to form AlN and contributes to the refinement of austenite crystal grains. Therefore, it is preferable to add at 0.0030% or more. However, when added in excess, not only is it difficult to secure the solid solution B, but also bubbles are generated in the steel ingot during solidification and deterioration of forgeability is caused, so the upper limit is made 0.0150%.
- the content of Al is specified as follows according to the amount of B.
- B- (10.8 / 14) N ⁇ 0.0003%: 0.010% ⁇ Al ⁇ 0.120%
- Al is an element necessary as a deoxidizing agent, and at the same time, in the present invention, it is necessary to secure solid solution B.
- solid solution B amount represents the remaining B amount after subtracting the stoichiometric amount of B that binds to N from the contained B (hereinafter also referred to as solid solution B amount). Yes. If this solid solution B amount is 0.0003% or more, it becomes possible to secure the solid solution B necessary for improving the hardenability.
- the Al content is set to a range of 0.010% or more and 0.120% or less.
- the balance of the above-described components is iron and inevitable impurities, and Ti among these impurities must be suppressed according to the upper limit shown below.
- Ti 0.005% or less Ti has a strong bonding force with N and forms TiN. However, since TiN exists in steel as a relatively large square inclusion, this becomes a starting point of fatigue, and in gears, surface fatigue such as pitching and bending fatigue strength at the root are reduced. Accordingly, in the present invention, Ti is an impurity, and it is preferable that Ti be as small as possible. Specifically, if it exceeds 0.005%, the above-mentioned adverse effects appear, so the Ti amount is limited to 0.005% or less.
- P and O are mentioned as inevitable impurities. That is, P is segregated at the grain boundary and causes the carburized layer and the internal toughness to be lowered. Specifically, when the content exceeds 0.020%, the above-described adverse effects appear, so the P content is preferably set to 0.020% or less.
- O is an element that exists as an oxide inclusion in steel and impairs fatigue strength. Like TiN inclusions, the lower the content, the lower the fatigue strength and toughness. Specifically, if it exceeds 0.0020%, the above-described adverse effects appear, so the O content is preferably 0.0020% or less.
- Nb 0.050% or less Nb may be added to refine crystal grains and strengthen grain boundaries to contribute to improving fatigue strength.
- Nb is added, it is preferably contained at least 0.010% or more.
- the effect is saturated at 0.050%, and addition of a large amount increases the cost, so the upper limit is preferably made 0.050%.
- V 0.200% or less
- V is an element that improves hardenability and increases temper softening resistance like Si and Cr, and also has an effect of forming carbonitrides and suppressing coarsening of crystal grains.
- it is preferable to add at 0.030% or more. Further, the effect is saturated at 0.200%, and the addition of a large amount increases the cost. Therefore, when added, the content is preferably 0.200% or less.
- a free cutting element such as Pb, Se, or Ca may be included as necessary.
- the suitable manufacturing conditions are as follows.
- a steel material having the above-described component composition is melt-cast to form a billet, and this billet is hot-rolled and then preformed to form a gear.
- it is machined or machined after forging to form a gear shape, and then carburized and quenched, and if necessary, the tooth surface is further polished to obtain a final product.
- shot peening or the like may be added.
- the carburizing and quenching treatment is preferably performed at a carburizing temperature of 900 to 1050 ° C., a quenching temperature of 800 to 900 ° C., and tempering within a range of 120 to 250 ° C.
- Table 2 shows the survey results for each of the survey items described above.
- the steels of the present invention (Nos. 1 to 15) have the same or better properties than SCr420 (No. 34) in both rotational bending and gear fatigue characteristics, and are superior to the comparative steels (No. 16 to 33). I understand.
- Comparative Steel No. 16 since the comparative steel No. 16 had a C content lower than the range of the present invention, the internal hardness was too low, and the rotational bending fatigue strength and the gear fatigue strength were reduced. Since the comparative steel No. 17 had a C content higher than the range of the present invention, the toughness of the core portion was reduced, and the rotary bending fatigue strength and the gear fatigue strength were reduced. In Comparative Steel No. 18, since the Si content was lower than the range of the present invention, the resistance to tempering softening decreased and the gear fatigue strength decreased. Comparative Steel No. 19 has a Si content lower than the range of the present invention and a Cr content higher than the range of the present invention.
- Comparative steel No. 20 has a Si content higher than the range of the present invention. Therefore, ferrite was generated inside, bending fatigue failure at the tooth root was likely to occur, and the gear fatigue strength was reduced.
- Comparative steel No. 21 has an Mn content lower than the range of the present invention. Therefore, the hardenability decreased and the effective effect layer depth became shallow, so that the rotational bending fatigue strength and the gear fatigue strength decreased. Since the comparative steel No.
- Comparative steel No. 22 has a Mn content higher than the range of the present invention, the Ms point of the carburized surface layer portion is lowered and the retained austenite amount is increased. Therefore, the surface hardness was lowered, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
- Comparative steel No. 23 has an S content higher than the range of the present invention. As a result, the amount of MnS generated as a starting point for fatigue failure increased, and the rotational bending fatigue strength and gear fatigue strength decreased.
- Comparative steel No. 24 has a Cr content lower than the range of the present invention. Therefore, the core hardness and the resistance to tempering softening decreased, and the rotational bending fatigue strength and the gear fatigue strength decreased. In Comparative Steel Nos.
- Comparative steel No. 27 has a B content lower than the range of the present invention. Therefore, the hardenability decreased and the effective effect layer depth became shallow, so that the rotational bending fatigue strength and the gear fatigue strength decreased.
- Comparative steel No. 28 has a B content higher than the range of the present invention. For this reason, the amount of BN produced that caused a decrease in toughness increased, and the rotational bending fatigue strength and gear fatigue strength decreased. In Comparative Steel No.
- Comparative steel No. 30 has a Sb content lower than the range of the present invention. For this reason, deboronation occurred during carburizing and the surface layer hardness was lowered, so that the rotational bending fatigue strength and the gear fatigue strength were reduced. Comparative steel No. 31 has an N content higher than the range of the present invention.
- Comparative steel No. 32 has a Ti content higher than the range of the present invention. As a result, fatigue failure due to the TiN starting point was likely to occur, and the rotary bending fatigue strength and gear fatigue strength were reduced. Comparative steel No. 33 is within the composition range of the present invention, but the Sb amount does not satisfy the prescribed formula (Sb ⁇ ⁇ Si / 2 + (Mn + Cr) / 5 ⁇ / 70), so the grain boundary oxide layer Is deep. Therefore, the surface layer hardness was lowered, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
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Abstract
Description
また、特許文献5には、Sbの添加により脱炭層厚みを抑制し、かつ従来の軟化焼鈍を施した鋼材と同等の冷間加工性を有する機械構造用鋼及びその製造方法が開示されている。 Patent Document 4 discloses a case hardening steel excellent in cold forgeability that suppresses the occurrence of an abnormal carburizing layer by addition of Sb and effectively suppresses coarsening of crystal grains by Ti-Mo carbide. Is disclosed.
Further, Patent Document 5 discloses a steel for machine structural use that suppresses the thickness of the decarburized layer by adding Sb and has a cold workability equivalent to that of a steel material that has been subjected to conventional soft annealing, and a method for manufacturing the same. .
まず、特許文献1および2に記載の技術では、いずれもNをTiNの形態で固定し、BがNと結合しないように考慮されている。しかしながら、TiNは比較的大きい角型の介在物として鋼中に存在するため、これが疲労の起点となり、歯車においてはピッチング等の面疲労や歯元の曲げ疲労強度を低下させる。また、角型のTiNは歯車の耐衝撃性を低下させ、歯車に衝撃的な荷重がかかった場合に歯車の折損につながる虞れがある。 However, each of the inventions described in Patent Documents 1 to 4 has the following problems.
First, in the techniques described in Patent Documents 1 and 2, N is fixed in the form of TiN, and it is considered that B does not combine with N. However, since TiN exists in steel as a relatively large square inclusion, this becomes a starting point of fatigue, and in gears, surface fatigue such as pitching and bending fatigue strength at the root are reduced. In addition, the square TiN reduces the impact resistance of the gear and may cause breakage of the gear when an impact load is applied to the gear.
(a)AlがNを固定したときに生成するAlNは、TiがNを固定して生成する比較的大型なTiN介在物とは異なり、微細な析出物となる。そのために、疲労強度や靱性を低下させる原因とならないばかりか、逆に結晶粒を微細化することによって疲労強度や靱性を向上させる効果を有する。
(b)Tiを添加せず、固溶Bの含有量を焼入れ性に効果のある3ppm以上確保するため、鋼中におけるAl-B-Nの化学平衡に基づき、Al含有量を厳密に制御する必要がある。
(c)Bはその反応性のゆえ、浸炭時に鋼材表面にて酸化や脱ボロン、窒化等の変化が生じ、表層部の焼入れ性を確保することが難しい。これに対し、Sbを添加することで上記反応を抑制することができる。
(d)Si、MnおよびCrは、焼戻し軟化抵抗の向上に有効であるが、過剰に添加すると、曲げ疲労および疲労亀裂の起点となる粒界酸化を助長する。これに対し、Si、MnおよびCrの含有量に応じてSbを添加することで上記反応を抑制することができる。 Inventors repeated earnest research in order to develop the case hardening steel excellent in fatigue resistance from the viewpoint mentioned above, and its manufacturing method. As a result, the following was found.
(A) AlN produced when Al fixes N is different from a relatively large TiN inclusion produced by Ti fixing N, and becomes a fine precipitate. Therefore, not only does it not cause a decrease in fatigue strength and toughness, but also has the effect of improving the fatigue strength and toughness by refining crystal grains.
(B) Without adding Ti, in order to secure a solid solution B content of 3 ppm or more effective in hardenability, the Al content is strictly controlled based on the chemical equilibrium of Al—BN in steel. There is a need.
(C) Due to the reactivity of B, changes such as oxidation, deboronization, and nitriding occur on the steel surface during carburization, and it is difficult to ensure the hardenability of the surface layer portion. On the other hand, the reaction can be suppressed by adding Sb.
(D) Si, Mn, and Cr are effective in improving the temper softening resistance, but when added in excess, promotes intergranular oxidation that becomes the starting point of bending fatigue and fatigue cracks. On the other hand, the reaction can be suppressed by adding Sb according to the contents of Si, Mn and Cr.
すなわち、本発明の要旨構成は、次のとおりである。
1.質量%で、
C:0.10~0.30%、
Si:0.10~1.20%、
Mn:0.30~1.50%、
S:0.010~0.030%、
Cr:0.10~1.00%、
B:0.0005~0.0050%、
Sb:0.005~0.020%および
N: 0.0150%以下
を、下記式を満足する範囲の下で含み、さらに、
Alを、B-(10.8/14)N≧0.0003%の場合に0.010%≦Al≦0.120%およびB-(10.8/14)N<0.0003%の場合に27/14[(N-(14/10.8)B+0.030]≦Al≦0.120%にて含有し、残部は鉄および不可避不純物からなり、
前記不可避不純物中のTiが、
Ti:0.005%以下
であることを特徴とする肌焼鋼。
記
Sb≧{Si/2+(Mn+Cr)/5}/70
The present invention is based on the above findings.
That is, the gist configuration of the present invention is as follows.
1. % By mass
C: 0.10 to 0.30%,
Si: 0.10 to 1.20%
Mn: 0.30-1.50%
S: 0.010 to 0.030%,
Cr: 0.10 to 1.00%,
B: 0.0005-0.0050%,
Sb: 0.005 to 0.020% and N: 0.0150% or less are included within a range satisfying the following formula,
When B- (10.8 / 14) N ≧ 0.0003%, 0.010% ≦ Al ≦ 0.120% and B- (10.8 / 14) N <0.0003%, 27/14 [((N− (14 / 10.8 ) B + 0.030] ≦ Al ≦ 0.120%, the balance is iron and inevitable impurities,
Ti in the inevitable impurities,
Ti: Case-hardened steel characterized by being 0.005% or less.
Sb ≧ {Si / 2 + (Mn + Cr) / 5} / 70
Nb:0.050%以下および
V:0.200%以下
のいずれか1種または2種を含有する前記1に記載の肌焼鋼。 2. Furthermore, the case hardening steel of said 1 containing the 1 type (s) or 2 types of Nb: 0.050% or less and V: 0.200% or less in the mass%.
まず、本発明において、鋼の成分組成を上記の範囲に限定した理由について説明する。なお、成分に関する「%」表示は特に断らない限り質量%を意味するものとする。
C: 0.10~0.30%
浸炭処理後の焼入れにより該焼入れ材の中心部(以下、単に芯部と示す)の硬度を高めるためには0.10%以上のCを必要とする。一方、含有量が0.30%を超えると芯部の靭性が低下する。従って、C量は0.10~0.30%の範囲に限定した。好ましくは0.15~0.25%の範囲である。 Hereinafter, the present invention will be specifically described.
First, the reason why the component composition of steel is limited to the above range in the present invention will be described. Unless otherwise specified, “%” in relation to ingredients means mass%.
C: 0.10 to 0.30%
In order to increase the hardness of the center portion (hereinafter simply referred to as a core portion) of the quenched material by quenching after carburizing treatment, C of 0.10% or more is required. On the other hand, if the content exceeds 0.30%, the toughness of the core part decreases. Therefore, the C content is limited to the range of 0.10 to 0.30%. Preferably it is 0.15 to 0.25% of range.
Siは、歯車等が転動中に到達すると推定される、200~300℃の温度域における軟化抵抗を高めるのに有効な元素である。また、浸炭時に粗大な炭化物の生成を抑制する効果も有しており、少なくとも0.10%の添加が不可欠である。一方で、Siはフェライト安定化元素であり、過剰な添加はAc3変態点を上昇させ、通常の焼入れ温度範囲において、炭素含有量の低い芯部でフェライトが出現し易くなり、歯元での曲げ疲労強度が低下するため、上限を1.20%とした。好ましくは0.20~0.60%の範囲である。 Si: 0.10 to 1.20%
Si is an element effective for increasing the softening resistance in a temperature range of 200 to 300 ° C., which is estimated to be reached during rolling of gears and the like. It also has an effect of suppressing the formation of coarse carbides during carburization, and at least 0.10% addition is essential. On the other hand, Si is a ferrite stabilizing element, and excessive addition raises the Ac 3 transformation point, and in the normal quenching temperature range, ferrite tends to appear in the core portion having a low carbon content, and at the tooth base. Since the bending fatigue strength decreases, the upper limit was made 1.20%. Preferably it is 0.20 to 0.60% of range.
Mnは、焼入性の向上に有効な元素であり、少なくとも0.30%の添加を必要とする。しかしながら、Mnは、浸炭異常層を形成し易く、また過剰な添加は残留オーステナイト量が過多となって硬さの低下を招くことから、上限を1.50%とした。好ましくは0.50~1.20%の範囲である。 Mn: 0.30 to 1.50%
Mn is an element effective for improving the hardenability and needs to be added at least 0.30%. However, Mn tends to form an abnormal carburization layer, and excessive addition causes an excessive amount of retained austenite and leads to a decrease in hardness, so the upper limit was made 1.50%. Preferably it is 0.50 to 1.20% of range.
Sは、Mnと硫化物を形成し、被削性を向上させる作用を有するため、少なくとも0.010%以上含有させる。一方、過剰な添加は、部品の疲労強度および靭性を低下させるため、上限を0.030%とした。 S: 0.010-0.030%
S has a function of forming sulfides with Mn and improving machinability, so it is contained at least 0.010% or more. On the other hand, excessive addition reduces the fatigue strength and toughness of the parts, so the upper limit was made 0.030%.
Crは、焼入性のみならず焼戻し軟化抵抗の向上にも有効な元素であり、含有量が0.10%に満たないとその添加効果に乏しい。一方、1.00%を超えると、浸炭異常層を形成し易くなる。さらに、焼入れ性が高くなりすぎて、歯車内部の靭性が劣化し、曲げ疲労強度が低下することになる。従って、Cr量は0.10~1.00%の範囲に限定した。好ましくは0.10~0.60%の範囲である。 Cr: 0.10 to 1.00%
Cr is an element effective for improving not only hardenability but also temper softening resistance, and if the content is less than 0.10%, its addition effect is poor. On the other hand, when it exceeds 1.00%, it becomes easy to form a carburized abnormal layer. Further, the hardenability becomes too high, the toughness inside the gear is deteriorated, and the bending fatigue strength is lowered. Therefore, the Cr content is limited to the range of 0.10 to 1.00%. Preferably it is 0.10 to 0.60% of range.
Bは、微量の添加により焼入れ性を確保するのに有効な元素であり、少なくとも0.0005%の添加を必要とする。一方、0.0050%を超えると、BNの量が増えてしまい、部品の疲労強度および靭性を低下させるため、B量は0.0005~0.0050%の範囲に限定した。好ましくは0.0010~0.0040%の範囲である。 B: 0.0005-0.0050%
B is an element effective for ensuring hardenability by adding a small amount, and needs to be added at least 0.0005%. On the other hand, if it exceeds 0.0050%, the amount of BN increases and the fatigue strength and toughness of the parts are reduced. Therefore, the amount of B is limited to the range of 0.0005 to 0.0050%. Preferably it is 0.0010 to 0.0040% of range.
Sbは、粒界への偏析傾向が強いため、浸炭処理中の脱ボロン、窒化(BN形成)等の表層反応を抑制し、焼入れ性を確保するために重要な元素である。その効果を得るには、少なくとも0.005%の添加が不可欠である。しかしながら、過剰な添加はコスト増につながるだけでなく、靭性を低下させるため、上限を0.020%とした。好ましくは0.005~0.015%の範囲である。 Sb: 0.005-0.020%
Since Sb has a strong tendency to segregate at grain boundaries, Sb is an important element for suppressing surface reaction such as deboronization and nitriding (BN formation) during carburizing treatment and ensuring hardenability. In order to obtain the effect, the addition of at least 0.005% is essential. However, excessive addition not only leads to an increase in cost but also reduces toughness, so the upper limit was made 0.020%. Preferably it is 0.005 to 0.015% of range.
Sb≧{Si/2+(Mn+Cr)/5}/70
の関係を満足させることが重要である。すなわち、上式は、粒界酸化層深さに影響を与える因子を示していて、SbがSi、MnおよびCr含有量に関する規定値を満たさない場合、粒界酸化の抑制効果に乏しく、疲労特性の低下を招くことになる。
ここで、粒界酸化とは、浸炭処理等の熱処理において鋼材の表層部の結晶粒界が内部酸化する現象であり、鋼中に選択酸化され易いSiやCr等が存在していると、その生成を助長する。粒界酸化部では上記の元素が酸化により消費されてしまうため、周辺部での焼入れ性低下に伴い硬度が低下し、そこを起点とした疲労破壊が起こりやすくなる。本発明では、粒界酸化の抑制作用を有するSbの添加量の下限をSi、Mn、Crの含有量に応じて上記式の右辺で示すように特定することによって、表層での焼入れ性を確保でき、疲労強度の低下を抑制できる。 Further, for Sb, the following formula relating to the contents of Si, Mn and Cr described above: Sb ≧ {Si / 2 + (Mn + Cr) / 5} / 70
It is important to satisfy this relationship. That is, the above equation shows the factors that affect the grain boundary oxide layer depth, and when Sb does not meet the specified values for Si, Mn, and Cr contents, the effect of suppressing grain boundary oxidation is poor, and the fatigue characteristics Will be reduced.
Here, grain boundary oxidation is a phenomenon in which the grain boundary of the surface layer portion of the steel material is internally oxidized in heat treatment such as carburizing treatment, and if there is Si or Cr which is easily oxidized in the steel, Contributes to generation. Since the above elements are consumed by oxidation in the grain boundary oxidation portion, the hardness is lowered with a decrease in the hardenability in the peripheral portion, and fatigue failure starting from the hardness tends to occur. In the present invention, by specifying the lower limit of the amount of Sb having the effect of suppressing grain boundary oxidation as indicated by the right side of the above formula according to the content of Si, Mn, Cr, ensuring hardenability in the surface layer It is possible to suppress a decrease in fatigue strength.
Nは、Alと結合してAlNを形成し、オーステナイト結晶粒の微細化に寄与する元素である。そのためには、0.0030%以上で添加することが好ましい。しかし、過剰に添加すると固溶Bの確保が困難になるだけでなく、凝固時の鋼塊に気泡が発生したり、鍛造性の劣化を招くため、上限を0.0150%とする。 N: 0.0150% or less N is an element that combines with Al to form AlN and contributes to the refinement of austenite crystal grains. Therefore, it is preferable to add at 0.0030% or more. However, when added in excess, not only is it difficult to secure the solid solution B, but also bubbles are generated in the steel ingot during solidification and deterioration of forgeability is caused, so the upper limit is made 0.0150%.
B-(10.8/14)N≧0.0003%の場合:0.010%≦Al≦0.120% Alは、脱酸剤として必要な元素であると同時に、本発明においては固溶Bを確保するためにも必要な元素である。ここで、「B-(10.8/14)N」は、含有Bのうち化学量論的にNと結合するB量を差し引いた残部のB量(以下、固溶B量ともいう)を表している。
この固溶B量が0.0003%以上であれば、焼入れ性向上に必要な固溶Bの確保が可能となる。この場合において、Al含有量が0.010%未満であると、脱酸が不十分になり、酸化物系介在物による疲労強度の低下をまねくことになる。一方、0.120%を超えてAlを添加すると、連続鋳造時のノズル詰まりの発生やアルミナクラスター介在物の発現により、靱性の低下を招く。よって、固溶B量が0.0003%以上のとき、Al含有量は0.010%以上0.120%以下の範囲とする。 The content of Al is specified as follows according to the amount of B.
When B- (10.8 / 14) N ≧ 0.0003%: 0.010% ≦ Al ≦ 0.120% Al is an element necessary as a deoxidizing agent, and at the same time, in the present invention, it is necessary to secure solid solution B. Element. Here, “B- (10.8 / 14) N” represents the remaining B amount after subtracting the stoichiometric amount of B that binds to N from the contained B (hereinafter also referred to as solid solution B amount). Yes.
If this solid solution B amount is 0.0003% or more, it becomes possible to secure the solid solution B necessary for improving the hardenability. In this case, if the Al content is less than 0.010%, deoxidation becomes insufficient, and the fatigue strength is reduced due to oxide inclusions. On the other hand, when Al is added exceeding 0.120%, the toughness is reduced due to the occurrence of nozzle clogging during continuous casting and the appearance of alumina cluster inclusions. Therefore, when the solid solution B content is 0.0003% or more, the Al content is set to a range of 0.010% or more and 0.120% or less.
この場合は、Nと比較的結合し易いAlの量を増やし、焼入れ性向上に寄与する固溶B量を確保する必要がある。そのために、Al含有量を27/14[(N-(14/10.8)B+0.030]%以上として0.0003%以上の固溶B量を確保する。なお、Alの上限は、上記と同様に0.120%とする。 When B- (10.8 / 14) N <0.0003%: 27/14 [(N- (14 / 10.8) B + 0.030] ≦ Al ≦ 0.120% On the other hand, when the amount of dissolved B is less than 0.0003% As long as there is no other alloying element that can be easily combined with N, the entire amount of N is combined with B, so that it is difficult to ensure solid solution B.
In this case, it is necessary to increase the amount of Al that is relatively easy to bond with N and to secure a solid solution B amount that contributes to improving the hardenability. Therefore, the Al content is 27/14 [(N- (14 / 10.8) B + 0.030]% or more, and a solid solution B amount of 0.0003% or more is ensured. %.
TiはNとの結合力が強く、TiNを形成する。しかし、TiNは比較的大きい角型の介在物として鋼中に存在するため、これが疲労の起点となり、歯車においてはピッチング等の面疲労や歯元の曲げ疲労強度を低下させる。従って、本発明においてTiは不純物であり、できるだけ少ない方がよい。具体的には、0.005%を超えると、上記弊害が現れるため、Ti量は0.005%以下に限定する。 Ti: 0.005% or less Ti has a strong bonding force with N and forms TiN. However, since TiN exists in steel as a relatively large square inclusion, this becomes a starting point of fatigue, and in gears, surface fatigue such as pitching and bending fatigue strength at the root are reduced. Accordingly, in the present invention, Ti is an impurity, and it is preferable that Ti be as small as possible. Specifically, if it exceeds 0.005%, the above-mentioned adverse effects appear, so the Ti amount is limited to 0.005% or less.
すなわち、Pは、粒界に偏析し、浸炭層及び内部の靭性を低下させる原因となるため、低いほど望ましい。具体的には、0.020%を超えると、上記弊害が現れるため、P量は0.020%以下とすることが好ましい。 In addition, P and O are mentioned as inevitable impurities.
That is, P is segregated at the grain boundary and causes the carburized layer and the internal toughness to be lowered. Specifically, when the content exceeds 0.020%, the above-described adverse effects appear, so the P content is preferably set to 0.020% or less.
Nb:0.050%以下
Nbは、結晶粒を微細化し、粒界を強化して疲労強度向上に寄与するため添加してもよく、添加する場合は、少なくとも0.010%以上で含有させることが好ましい。一方、その効果は0.050%で飽和し、かつ多量の添加はコスト増になるため、上限を0.050%とすることが好ましい。 The above is the basic component composition of the present invention, but when further improving the characteristics, either one or two of Nb and V may be contained.
Nb: 0.050% or less Nb may be added to refine crystal grains and strengthen grain boundaries to contribute to improving fatigue strength. When Nb is added, it is preferably contained at least 0.010% or more. On the other hand, the effect is saturated at 0.050%, and addition of a large amount increases the cost, so the upper limit is preferably made 0.050%.
Vは、焼入れ性を向上させると共にSiやCrと同じく焼戻し軟化抵抗を高める元素であり、炭窒化物を形成して結晶粒の粗大化を抑制する効果も有する。このような効果を発揮させるためには、0.030%以上で添加することが好ましい。また、その効果は0.200%で飽和し、かつ多量の添加はコスト増になるため、添加する場合は、0.200%以下とすることが好ましい。
なお、被削性を向上させるためには、必要に応じて、Pb、Se、Ca等の快削元素を含有させてもよい。 V: 0.200% or less V is an element that improves hardenability and increases temper softening resistance like Si and Cr, and also has an effect of forming carbonitrides and suppressing coarsening of crystal grains. In order to exert such an effect, it is preferable to add at 0.030% or more. Further, the effect is saturated at 0.200%, and the addition of a large amount increases the cost. Therefore, when added, the content is preferably 0.200% or less.
In order to improve machinability, a free cutting element such as Pb, Se, or Ca may be included as necessary.
前記した成分組成からなる鋼素材を溶解鋳造してビレットとし、このビレットを熱間圧延後、歯車とするための予備成形を行う。次に、機械加工、あるいは鍛造後に機械加工を行い歯車形状とした後、浸炭焼入れ処理を施し、必要に応じて更に歯面に研磨加工を施して最終製品とする。更には、ショットピーニング等を付加しても良い。浸炭焼入れ処理は、浸炭温度900~1050℃、焼入れ温度800~900℃とし、焼戻しは120~250℃の範囲とすることが好ましい。 Although there is no restriction | limiting in particular about the manufacturing conditions at the time of producing the machine structural component from the case hardening steel based on this invention, The suitable manufacturing conditions are as follows.
A steel material having the above-described component composition is melt-cast to form a billet, and this billet is hot-rolled and then preformed to form a gear. Next, it is machined or machined after forging to form a gear shape, and then carburized and quenched, and if necessary, the tooth surface is further polished to obtain a final product. Furthermore, shot peening or the like may be added. The carburizing and quenching treatment is preferably performed at a carburizing temperature of 900 to 1050 ° C., a quenching temperature of 800 to 900 ° C., and tempering within a range of 120 to 250 ° C.
発明鋼、比較鋼及びSCr420の20mmφ丸棒に、浸炭焼入れ・焼戻し処理を施した後に切断し、この切断面において最大となる粒界酸化層深さを、エッチングすることなく光学顕微鏡で400倍の倍率にて測定した。
また、同じ断面の硬度分布を測定し、ビッカース硬さで550HVとなる表面からの深さを有効硬化層深さとした。表面硬度は、丸棒表面のビッカース硬さ(HV10kgf)10点の平均値とした。さらに、表層より5mm深さ位置のビッカース硬さ(HV10kgf)5点の平均値を内部硬度と規定した。 [Grain boundary oxide layer depth, effective hardened layer depth, surface hardness, internal hardness]
Invented steel, comparative steel and SCr420 20mmφ round bar were cut after carburizing quenching and tempering treatment, and the maximum grain boundary oxide layer depth in this cut surface was 400 times by optical microscope without etching. Measured with magnification.
The hardness distribution of the same cross section was measured, and the depth from the surface where the Vickers hardness was 550 HV was defined as the effective hardened layer depth. The surface hardness was an average value of 10 points of Vickers hardness (HV 10 kgf) on the surface of the round bar. Furthermore, the average value of five points of Vickers hardness (HV 10 kgf) at a depth of 5 mm from the surface layer was defined as the internal hardness.
直径32mmの丸棒鋼から、平行部が圧延方向と一致するように、図2に示す寸法および形状の平行部直径8mmの試験片を採取し、平行部にこれと直角方向の深さ2mmの切欠き(切欠き係数:1.56)を全周に付与した回転曲げ疲労試験片を作製した。得られた試験片に対して、浸炭焼入れ・焼戻し処理を行った後、小野式回転曲げ疲労試験機を用い、回転数:3000rpmで回転曲げ疲労試験を実施し、107回を疲労限度として、回転曲げ疲労強度を測定した。 [Rotating bending fatigue characteristics]
From a round steel bar with a diameter of 32 mm, a test piece with a parallel part diameter of 8 mm having the dimensions and shape shown in Fig. 2 is taken so that the parallel part coincides with the rolling direction. A rotating bending fatigue test piece having notches (notch coefficient: 1.56) all around was prepared. The obtained test pieces, after carburizing quenching and tempering process, using a fatigue tester Ono-type rotating bending, rotation speed: conducted rotary bending fatigue test at 3000 rpm, 10 7 times as fatigue limit, The rotational bending fatigue strength was measured.
直径70mmの丸棒を熱間鍛造後に機械加工して、モジュール2.5、ピッチ直径80mmのハスバ歯車を作製した。得られた試験片に対して、動力循環式歯車疲労試験機を使用して、80℃のトランスアクスルオイルを潤滑に用い、所定のトルクをかけて回転数:3000rpmにて試験を実施し、107回を疲労限度として、歯車疲労強度を測定した。 [Gear fatigue characteristics]
A round bar with a diameter of 70 mm was machined after hot forging to produce a helical gear with a module 2.5 and a pitch diameter of 80 mm. Using the power cycle type gear fatigue tester, the test piece obtained was tested at 80 ° C. transaxle oil for lubrication, applying a predetermined torque and rotating at 3000 rpm. The gear fatigue strength was measured with 7 times as the fatigue limit.
上記した調査項目毎の調査結果を、表2に示す。本発明鋼(No.1~15)は、回転曲げ/歯車疲労特性共にSCr420(No.34)と同等以上の特性が得られており、比較鋼(No.16~33)より優れていることがわかる。 [Investigation result]
Table 2 shows the survey results for each of the survey items described above. The steels of the present invention (Nos. 1 to 15) have the same or better properties than SCr420 (No. 34) in both rotational bending and gear fatigue characteristics, and are superior to the comparative steels (No. 16 to 33). I understand.
比較鋼No.17は、C含有量が本発明範囲より高いために、芯部の靭性が低下し、回転曲げ疲労強度および歯車疲労強度が低下した。
比較鋼No.18は、Si含有量が本発明の範囲よりも低いために、耐焼戻し軟化抵抗が低下し、歯車疲労強度が低下した。
比較鋼No.19は、Si含有量が本発明の範囲よりも低くかつCr含有量が本発明の範囲より高い。そのため、浸炭表層部のMs点が低下し、残留オーステナイト量が増加する。よって、表層硬度が低くなり、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.20は、Si含有量が本発明の範囲よりも高い。そのため、内部にフェライトが発生し、歯元での曲げ疲労破壊が起こりやすくなり、歯車疲労強度が低下した。
比較鋼No.21は、Mn含有量が本発明範囲より低い。そのため、焼入れ性が低下し、有効効果層深さが浅くなったため、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.22は、Mn含有量が本発明の範囲より高いために、浸炭表層部のMs点が低下し、残留オーステナイト量が増加する。よって、表面硬度が低くなり、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.23は、S含有量が本発明範囲より高い。そのため、疲労破壊の起点となるMnSの生成量が多くなり、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.24は、Cr含有量が本発明の範囲より低い。そのため、芯部硬度及び耐焼戻し軟化抵抗が低下し、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.25および26は、Cr含有量が本発明の範囲より高いために、浸炭表層部のMs点が低下し、残留オーステナイト量が増加する。よって、表層硬度が低くなり、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.27は、B含有量が本発明の範囲より低い。そのため、焼入れ性が低下し、有効効果層深さが浅くなったため、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.28は、B含有量が本発明の範囲より高い。そのため、靭性の低下を招くBNの生成量が多くなり、回転曲げ疲労強度および歯車疲労強度が低下した。
比較鋼No.29は、Al含有量が本発明で規定した式(27/14[(N-(14 /10.8)B+0.030]≦Al≦0.120%)から算出される下限値より低い。そのため、焼入れ性向上に寄与する固溶B量が確保できず、有効効果層深さが浅く、内部硬度も低くなったため、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.30は、Sb含有量が本発明範囲より低い。そのため、浸炭時に脱ボロンが生じてしまい、表層硬度が低くなったため、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.31は、N含有量が本発明の範囲より高い。その結果、焼入れ性向上に寄与する固溶B量が確保できず、有効効果層深さが浅く、内部硬度も低くなったため、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.32は、Ti含有量が本発明の範囲より高い。そのため、TiN起点による疲労破壊が起こりやすくなり、回転曲げ疲労強度と歯車疲労強度が低下した。
比較鋼No.33は、本発明成分範囲内であるが、Sb量が規定式(Sb≧{Si/2+(Mn+Cr)/5}/70)を満たしていないため、粒界酸化層が深い。よって、表層硬度が低くなり、回転曲げ疲労強度と歯車疲労強度が低下した。 That is, since the comparative steel No. 16 had a C content lower than the range of the present invention, the internal hardness was too low, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
Since the comparative steel No. 17 had a C content higher than the range of the present invention, the toughness of the core portion was reduced, and the rotary bending fatigue strength and the gear fatigue strength were reduced.
In Comparative Steel No. 18, since the Si content was lower than the range of the present invention, the resistance to tempering softening decreased and the gear fatigue strength decreased.
Comparative Steel No. 19 has a Si content lower than the range of the present invention and a Cr content higher than the range of the present invention. For this reason, the Ms point of the carburized surface layer portion decreases and the amount of retained austenite increases. Therefore, the surface layer hardness was lowered, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
Comparative steel No. 20 has a Si content higher than the range of the present invention. Therefore, ferrite was generated inside, bending fatigue failure at the tooth root was likely to occur, and the gear fatigue strength was reduced.
Comparative steel No. 21 has an Mn content lower than the range of the present invention. Therefore, the hardenability decreased and the effective effect layer depth became shallow, so that the rotational bending fatigue strength and the gear fatigue strength decreased.
Since the comparative steel No. 22 has a Mn content higher than the range of the present invention, the Ms point of the carburized surface layer portion is lowered and the retained austenite amount is increased. Therefore, the surface hardness was lowered, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
Comparative steel No. 23 has an S content higher than the range of the present invention. As a result, the amount of MnS generated as a starting point for fatigue failure increased, and the rotational bending fatigue strength and gear fatigue strength decreased.
Comparative steel No. 24 has a Cr content lower than the range of the present invention. Therefore, the core hardness and the resistance to tempering softening decreased, and the rotational bending fatigue strength and the gear fatigue strength decreased.
In Comparative Steel Nos. 25 and 26, since the Cr content is higher than the range of the present invention, the Ms point of the carburized surface layer portion decreases and the retained austenite amount increases. Therefore, the surface layer hardness was lowered, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
Comparative steel No. 27 has a B content lower than the range of the present invention. Therefore, the hardenability decreased and the effective effect layer depth became shallow, so that the rotational bending fatigue strength and the gear fatigue strength decreased.
Comparative steel No. 28 has a B content higher than the range of the present invention. For this reason, the amount of BN produced that caused a decrease in toughness increased, and the rotational bending fatigue strength and gear fatigue strength decreased.
In Comparative Steel No. 29, the Al content is lower than the lower limit value calculated from the formula (27/14 [(N− (14 / 10.8) B + 0.030] ≦ Al ≦ 0.120%) defined in the present invention. Rotational bending fatigue strength and gear fatigue strength decreased because the amount of solute B that contributed to improving hardenability could not be secured, the effective effect layer depth was shallow, and the internal hardness was low.
Comparative steel No. 30 has a Sb content lower than the range of the present invention. For this reason, deboronation occurred during carburizing and the surface layer hardness was lowered, so that the rotational bending fatigue strength and the gear fatigue strength were reduced.
Comparative steel No. 31 has an N content higher than the range of the present invention. As a result, the amount of solute B contributing to the improvement of hardenability could not be secured, the effective effect layer depth was shallow, and the internal hardness was low, so that the rotational bending fatigue strength and the gear fatigue strength were reduced.
Comparative steel No. 32 has a Ti content higher than the range of the present invention. As a result, fatigue failure due to the TiN starting point was likely to occur, and the rotary bending fatigue strength and gear fatigue strength were reduced.
Comparative steel No. 33 is within the composition range of the present invention, but the Sb amount does not satisfy the prescribed formula (Sb ≧ {Si / 2 + (Mn + Cr) / 5} / 70), so the grain boundary oxide layer Is deep. Therefore, the surface layer hardness was lowered, and the rotational bending fatigue strength and the gear fatigue strength were reduced.
Claims (2)
- 質量%で、
C:0.10~0.30%、
Si:0.10~1.20%、
Mn:0.30~1.50%、
S:0.010~0.030%、
Cr:0.10~1.00%、
B:0.0005~0.0050%、
Sb:0.005~0.020%および
N: 0.0150%以下
を、下記式を満足する範囲の下で含み、さらに、
Alを、B-(10.8/14)N≧0.0003%の場合に0.010%≦Al≦0.120%およびB-(10.8/14)N<0.0003%の場合に27/14[(N-(14/10.8)B+0.030]≦Al≦0.120%にて含有し、残部は鉄および不可避不純物からなり、
前記不可避不純物中のTiが、
Ti:0.005%以下
であることを特徴とする肌焼鋼。
記
Sb≧{Si/2+(Mn+Cr)/5}/70 % By mass
C: 0.10 to 0.30%,
Si: 0.10 to 1.20%
Mn: 0.30-1.50%
S: 0.010 to 0.030%,
Cr: 0.10 to 1.00%,
B: 0.0005-0.0050%,
Sb: 0.005 to 0.020% and N: 0.0150% or less are included within a range satisfying the following formula,
When B- (10.8 / 14) N ≧ 0.0003%, 0.010% ≦ Al ≦ 0.120% and B- (10.8 / 14) N <0.0003%, 27/14 [((N− (14 / 10.8 ) B + 0.030] ≦ Al ≦ 0.120%, the balance is iron and inevitable impurities,
Ti in the inevitable impurities,
Ti: Case-hardened steel characterized by being 0.005% or less.
Sb ≧ {Si / 2 + (Mn + Cr) / 5} / 70 - さらに、質量%で
Nb:0.050%以下および
V:0.200%以下
のいずれか1種または2種を含有する請求項1に記載の肌焼鋼。 Furthermore, the case hardening steel of Claim 1 which contains any 1 type or 2 types of Nb: 0.050% or less and V: 0.200% or less in the mass%.
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009108340A (en) * | 2007-10-26 | 2009-05-21 | Nippon Steel Corp | Quenching steel excellent in machinability and hardenability |
JP2011184768A (en) * | 2010-03-10 | 2011-09-22 | Kobe Steel Ltd | High strength case hardening steel component and method for producing the same |
JP2012140675A (en) * | 2010-12-28 | 2012-07-26 | Jfe Steel Corp | Case-hardening steel excellent in cold-workability, and high fatigue-resistant strength carburized material |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5770261A (en) | 1980-10-18 | 1982-04-30 | Sumitomo Metal Ind Ltd | Boronic case hardening steel with reduced carburized abnormal layer |
JPS58120719A (en) | 1982-01-08 | 1983-07-18 | Kobe Steel Ltd | Manufacture of case hardening b steel |
JPH05171262A (en) * | 1991-12-18 | 1993-07-09 | Kawasaki Steel Corp | Manufacture of wire rod or bar steel for case hardened product |
JPH07261A (en) | 1993-06-11 | 1995-01-06 | Matsushita Electric Works Ltd | Household furniture |
JP3954437B2 (en) | 2002-05-30 | 2007-08-08 | 愛知製鋼株式会社 | Method for producing case-hardened boron steel to prevent abnormal grain growth of crystal grains |
CN100436628C (en) | 2003-01-17 | 2008-11-26 | 杰富意钢铁株式会社 | Steel product for induction hardening, induction-hardened member using the same, and methods for producing them |
WO2004065646A1 (en) | 2003-01-17 | 2004-08-05 | Jfe Steel Corporation | Steel product for induction hardening, induction-hardened member using the same, and methods for producing them |
JP4057930B2 (en) | 2003-02-21 | 2008-03-05 | 新日本製鐵株式会社 | Machine structural steel excellent in cold workability and method for producing the same |
JP4709944B2 (en) | 2009-01-16 | 2011-06-29 | 新日本製鐵株式会社 | Case-hardened steel, carburized parts, and method for producing case-hardened steel |
KR101367350B1 (en) * | 2009-04-06 | 2014-02-26 | 신닛테츠스미킨 카부시키카이샤 | Steel for case hardening which has excellent cold workability and machinability and which exhibits excellent fatigue characteristics after carburizing and quenching, and process for production of same |
JP5458649B2 (en) * | 2009-04-28 | 2014-04-02 | Jfeスチール株式会社 | High carbon hot rolled steel sheet and manufacturing method thereof |
JP2011164768A (en) | 2010-02-05 | 2011-08-25 | Yokogawa Denshikiki Co Ltd | Security system |
JP4883240B1 (en) * | 2010-08-04 | 2012-02-22 | Jfeスチール株式会社 | Steel sheet for hot press and method for producing hot press member using the same |
JP5672849B2 (en) * | 2010-08-20 | 2015-02-18 | Jfeスチール株式会社 | Steel sheet for hot pressing, method for manufacturing the same, and method for manufacturing hot pressed members using the same |
JP5649887B2 (en) | 2010-09-16 | 2015-01-07 | Jfeスチール株式会社 | Case-hardened steel and method for producing the same |
JP5432105B2 (en) | 2010-09-28 | 2014-03-05 | 株式会社神戸製鋼所 | Case-hardened steel and method for producing the same |
WO2012046779A1 (en) | 2010-10-06 | 2012-04-12 | 新日本製鐵株式会社 | Case hardened steel and method for producing the same |
JP5884151B2 (en) * | 2010-11-25 | 2016-03-15 | Jfeスチール株式会社 | Steel sheet for hot press and method for producing hot press member using the same |
JP6020589B2 (en) | 2013-07-02 | 2016-11-02 | Jfeスチール株式会社 | Manufacturing method of hot press member |
-
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009108340A (en) * | 2007-10-26 | 2009-05-21 | Nippon Steel Corp | Quenching steel excellent in machinability and hardenability |
JP2011184768A (en) * | 2010-03-10 | 2011-09-22 | Kobe Steel Ltd | High strength case hardening steel component and method for producing the same |
JP2012140675A (en) * | 2010-12-28 | 2012-07-26 | Jfe Steel Corp | Case-hardening steel excellent in cold-workability, and high fatigue-resistant strength carburized material |
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